Journal
NATURE STRUCTURAL & MOLECULAR BIOLOGY
Volume 24, Issue 11, Pages 986-+Publisher
NATURE PUBLISHING GROUP
DOI: 10.1038/nsmb.3484
Keywords
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Funding
- UK Biotechnology and Biological Sciences Research Council [BB/M024709/1]
- UK Medical Research Council [MR/L009609/1, MC_UP_1201/15]
- Human Frontier Science Program [RGP0065/2014]
- Wellcome Trust [105247/Z/14/Z, 084655/Z/08/Z]
- Wellcome Trust Core Award [090532/Z/09/Z]
- Biotechnology and Biological Sciences Research Council [BB/M024709/1] Funding Source: researchfish
- Medical Research Council [MR/L009609/1, MC_UP_1201/15] Funding Source: researchfish
- BBSRC [BB/M024709/1] Funding Source: UKRI
- MRC [MR/L009609/1, MC_UP_1201/15] Funding Source: UKRI
- Wellcome Trust [105247/Z/14/Z, 084655/Z/08/Z] Funding Source: Wellcome Trust
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Type A gamma-aminobutyric acid receptors (GABA(A)Rs) are the principal mediators of inhibitory neurotransmission in the human brain. Endogenous neurosteroids interact with GABA(A)Rs to regulate acute and chronic anxiety and are potent sedative, analgesic, anticonvulsant and anesthetic agents. Their mode of binding and mechanism of receptor potentiation, however, remain unknown. Here we report crystal structures of a chimeric GABA(A)R construct in apo and pregnanolone-bound states. The neurosteroid-binding site is mechanically coupled to the helices lining the ion channel pore and modulates the desensitization-gate conformation. We demonstrate that the equivalent site is responsible for physiological, heteromeric GABA(A)R potentiation and explain the contrasting modulatory properties of 3 alpha versus 3 beta neurosteroid epimers. These results illustrate how peripheral lipid ligands can regulate the desensitization gate of GABA(A)Rs, a process of broad relevance to pentameric ligand-gated ion channels.
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